Results 101 to 110 of about 19,520 (191)

A copper-catalyzed arylation of tryptamines for the direct synthesis of aryl pyrroloindolines [PDF]

open access: yes, 2012
An operationally simple, copper-catalyzed arylation of N-tosyltryptamines provides direct access to C3-aryl pyrroloindolines. A range of electron-donating and electron-withdrawing substituents is tolerated on both the indole backbone and the aryl ...
Chuang, Kangway V.   +2 more
core   +1 more source

Phosphine-free palladium-catalysed direct C2-arylation of benzothiophenes with aryl bromides [PDF]

open access: yes, 2013
Copies of 1H and 13C NMR spectra of new compounds are available (attached file).International audienceLigand-free Pd(OAc)2 was found to catalyse very efficiently the direct C2-arylation of benzothiophene derivatives under low catalyst concentration.
Bruneau, Christian   +2 more
core   +3 more sources

Palladium single-atom/cluster cocatalyst supported on non-enzymatic browning glucose breaks the activity-selectivity trade-off in C(sp3)-H arylation

open access: yesCommunications Chemistry
Using Pd homogeneous catalysts for direct C–H arylation is an attractive approach for synthesizing natural products and organic functional materials, but limitations in terms of cost and catalyst recovery could be alleviated by alternative heterogeneous ...
Xiaojie He   +6 more
doaj   +1 more source

Site-selective arylations of nature-inspired flavonoids or steroidal phenols via C—H or O—H activation

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry
Phenols are important structural elements of natural products and pharmaceuticals. Due to their versatile chemical transformability, phenols are frequently used building blocks in medicinal chemistry.
Rebeka Ignácz   +8 more
doaj   +1 more source

Push-pull bithiophene azo-chromophores bearing thiazole and benzothiazole acceptor moieties: synthesis and evaluation of their redox and nonlinear optical properties [PDF]

open access: yes, 2011
Three series of bithiophene azo dyes functionalized with thiazol-2-yl or benzothiazol-2-yl-diazene acceptor moieties were synthesized through azo coupling reaction using 2,2´-bithiophene, 5-alkoxy-2,2´-bithiophenes, 5-N,N-dialkylamino-2,2´-bithiophenes ...
Belsley, M.   +3 more
core   +1 more source

Birch reductive arylation by mechanochemical anionic activation of polycyclic aromatic compounds

open access: yesNature Communications
Birch reduction is a well-known process for transforming aromatic compounds. The reduction of aromatic rings using alkali metals produces anionic species that react with protons or electrophiles.
Yoshifumi Toyama   +3 more
doaj   +1 more source

Integrated catalysis opens new arylation pathways via regiodivergent enzymatic C–H activation

open access: yesNature Communications, 2016
Biocatalysis and metal catalysis often provide complimentary reactivities and selectivities. Here, the authors exploit the regioselectivity of an enzymatic C–H activation followed by palladium catalysed carbon-carbon bond formation in one pot, with ...
Jonathan Latham   +6 more
doaj   +1 more source

Palladium-catalyzed C(sp^3)–H arylation of lactic acid: efficient synthesis of chiral β-aryl-α-hydroxy acids [PDF]

open access: yes, 2016
A Pd-catalyzed arylation of lactic acid employing 8-aminoquinoline as the directing group has been reported. The protocol is found to be compatible with a broad range of synthetically useful functional groups, thus providing a practical route to chiral β-
Chen, Kai   +3 more
core   +1 more source

Catalytic enantioselective synthesis of quaternary carbon stereocentres. [PDF]

open access: yes, 2014
Quaternary carbon stereocentres-carbon atoms to which four distinct carbon substituents are attached-are common features of molecules found in nature. However, before recent advances in chemical catalysis, there were few methods of constructing single ...
Overman, Larry E, Quasdorf, Kyle W
core  

Highly selective electrochemical hydrogenation of alkynes: Rapid construction of mechanochromic materials [PDF]

open access: yes, 2019
Electrochemical hydrogenation has emerged as an environmentally benign and operationally simple alternative to traditional catalytic reduction of organic compounds.
Ge, Haibo, Li, Bijin
core   +1 more source

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